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dc.contributor.authorAl-Muhsen, Saleh
dc.contributor.authorCasanova, Jean-Laurent
dc.contributor.authorAbel, Laurent
dc.contributor.authorGrant, Audrey V.
dc.contributor.authorBoisson-Dupuis, Stephanie
dc.contributor.authorHerquelot, Eleonore
dc.contributor.authorde Beaucoudrey, Ludovic
dc.contributor.authorFilipe-Santos, Orchidee
dc.contributor.authorCamcioglu, Yildiz
dc.contributor.authorPalanduz, Ayşe
dc.contributor.authorNolan, Daniel K.
dc.contributor.authorFeinberg, Jacqueline
dc.contributor.authorBoland, Anne
dc.contributor.authorSanal, Ozden
dc.contributor.authorKilic, Sara Sebnem
dc.contributor.authorBustamante, Jacinta
dc.date.accessioned2021-03-05T13:58:14Z
dc.date.available2021-03-05T13:58:14Z
dc.date.issued2011
dc.identifier.citationGrant A. V. , Boisson-Dupuis S., Herquelot E., de Beaucoudrey L., Filipe-Santos O., Nolan D. K. , Feinberg J., Boland A., Al-Muhsen S., Sanal O., et al., "Accounting for genetic heterogeneity in homozygosity mapping: application to Mendelian susceptibility to mycobacterial disease", JOURNAL OF MEDICAL GENETICS, cilt.48, ss.567-571, 2011
dc.identifier.issn0022-2593
dc.identifier.othervv_1032021
dc.identifier.otherav_b4d3c1cb-435f-4889-9afa-764bd5c350db
dc.identifier.urihttp://hdl.handle.net/20.500.12627/120407
dc.identifier.urihttps://doi.org/10.1136/jmg.2011.089128
dc.description.abstractIntroduction Genome-wide homozygosity mapping is a powerful method for locating rare recessive Mendelian mutations. However, statistical power decreases dramatically in the presence of genetic heterogeneity.
dc.language.isoeng
dc.subjectTemel Bilimler
dc.subjectGENETİK VE HAYAT
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.titleAccounting for genetic heterogeneity in homozygosity mapping: application to Mendelian susceptibility to mycobacterial disease
dc.typeMakale
dc.relation.journalJOURNAL OF MEDICAL GENETICS
dc.contributor.departmentInstitut National de la Sante et de la Recherche Medicale (Inserm) , ,
dc.identifier.volume48
dc.identifier.issue8
dc.identifier.startpage567
dc.identifier.endpage571
dc.contributor.firstauthorID26732


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